open access

Vol 55, No 3 (2017)
Original paper
Submitted: 2016-10-19
Accepted: 2017-07-25
Published online: 2017-08-03
Get Citation

Morphological alterations in the jejunal mucosa of aged rats and the possible protective role of green tea

Zeinab A. Hassan, Agata Zauszkiewicz-Pawlak1, Shaimaa A. Abdelrahman, Sami Algaidi, Maha Desouky, Sally M. Shalaby
·
Pubmed: 28813122
·
Folia Histochem Cytobiol 2017;55(3):124-139.
Affiliations
  1. Department of Histology, Medical University of Gdansk, Gdansk, Poland

open access

Vol 55, No 3 (2017)
ORIGINAL PAPERS
Submitted: 2016-10-19
Accepted: 2017-07-25
Published online: 2017-08-03

Abstract

Introduction. Gastrointestinal disorders become more prevalent with ageing. This study is aimed to describe morphological changes that occur in the jejunal mucosa of male albino rats as a result of ageing and the protec­tive effect of green tea (GT) extract.

Material and methods. The experiment was performed on sixty rats: thirty young-adult (6-month old, body mass 200–220 g) and thirty old (24-month-old, body mass 220–260 g) animals. Each group was further divided into two subgroups (n = 15 each): control rats and GT-treated rats that received 1.5 mL (300 mg/kg/day) of GT extract for 14 weeks by oral gavage. Sections of the jejunum were stained with hematoxylin and eosin, periodic acid Schiff, toluidine blue and Mallory trichrome methods. The presence of proliferating cell nuclear antigen (PCNA)- and CD68-positive cells was evaluated by immunohistochemical staining. Ultrathin sections were prepared and examined by a transmission electron microscope (TEM).

Results. Jejunal sections of the old control rats showed distortion of submucosa and attenuated muscularis externa with decreased height of intestinal villi. The villi also showed partial loss of acidophilic brush border with wide spaces between enterocytes. Swollen, short, blunt or broad villi with abundant mononuclear cell infiltration of lamina propria and congested blood vessels were evident both by light and electron microscopy. The number of PCNA- and CD68-positive cells in jejunal mucosa of old rats was higher than in young rats. The activity of glutathione peroxidase (GPX) and total antioxidant capacity (TAC) in the mucosa of old control rats were lower, whereas malondialdehyde (MDA) levels were higher in the jejunal homogenates of old rats as compared to young control rats. Administration of GT extract protected the jejunal mucosa from age-related changes by restoring its histological structure. The treatment of old rats with GT extract significantly decreased MDA levels in the jejunum and increased TAC and GPX activity.

Conclusions. The age-related changes of the morphology of rat jejunum could be ameliorated by prolonged supplementation of the green tea extract.

Abstract

Introduction. Gastrointestinal disorders become more prevalent with ageing. This study is aimed to describe morphological changes that occur in the jejunal mucosa of male albino rats as a result of ageing and the protec­tive effect of green tea (GT) extract.

Material and methods. The experiment was performed on sixty rats: thirty young-adult (6-month old, body mass 200–220 g) and thirty old (24-month-old, body mass 220–260 g) animals. Each group was further divided into two subgroups (n = 15 each): control rats and GT-treated rats that received 1.5 mL (300 mg/kg/day) of GT extract for 14 weeks by oral gavage. Sections of the jejunum were stained with hematoxylin and eosin, periodic acid Schiff, toluidine blue and Mallory trichrome methods. The presence of proliferating cell nuclear antigen (PCNA)- and CD68-positive cells was evaluated by immunohistochemical staining. Ultrathin sections were prepared and examined by a transmission electron microscope (TEM).

Results. Jejunal sections of the old control rats showed distortion of submucosa and attenuated muscularis externa with decreased height of intestinal villi. The villi also showed partial loss of acidophilic brush border with wide spaces between enterocytes. Swollen, short, blunt or broad villi with abundant mononuclear cell infiltration of lamina propria and congested blood vessels were evident both by light and electron microscopy. The number of PCNA- and CD68-positive cells in jejunal mucosa of old rats was higher than in young rats. The activity of glutathione peroxidase (GPX) and total antioxidant capacity (TAC) in the mucosa of old control rats were lower, whereas malondialdehyde (MDA) levels were higher in the jejunal homogenates of old rats as compared to young control rats. Administration of GT extract protected the jejunal mucosa from age-related changes by restoring its histological structure. The treatment of old rats with GT extract significantly decreased MDA levels in the jejunum and increased TAC and GPX activity.

Conclusions. The age-related changes of the morphology of rat jejunum could be ameliorated by prolonged supplementation of the green tea extract.

Get Citation

Keywords

rat; aging; jejunal mucosa; morphology; green tea; PCNA, CD68; IHC; TEM

Supp./Additional Files (1)
Supplementary Figure 1
View
3MB
About this article
Title

Morphological alterations in the jejunal mucosa of aged rats and the possible protective role of green tea

Journal

Folia Histochemica et Cytobiologica

Issue

Vol 55, No 3 (2017)

Article type

Original paper

Pages

124-139

Published online

2017-08-03

Page views

1851

Article views/downloads

1812

DOI

10.5603/FHC.a2017.0012

Pubmed

28813122

Bibliographic record

Folia Histochem Cytobiol 2017;55(3):124-139.

Keywords

rat
aging
jejunal mucosa
morphology
green tea
PCNA
CD68
IHC
TEM

Authors

Zeinab A. Hassan
Agata Zauszkiewicz-Pawlak
Shaimaa A. Abdelrahman
Sami Algaidi
Maha Desouky
Sally M. Shalaby

References (51)
  1. Saffrey MJ. Aging of the mammalian gastrointestinal tract: a complex organ system. Age (Dordr). 2014; 36(3): 9603.
  2. Wang Li, Li J, Li Q, et al. Morphological changes of cell proliferation and apoptosis in rat jejunal mucosa at different ages. World J Gastroenterol. 2003; 9(9): 2060–2064.
  3. Williams JM, Duckworth CA, Burkitt MD, et al. Epithelial cell shedding and barrier function: a matter of life and death at the small intestinal villus tip. Vet Pathol. 2015; 52(3): 445–455.
  4. Wong WM, Wright NA. Cell proliferation in gastrointestinal mucosa. J Clin Pathol. 1999; 52(5): 321–333.
  5. Firth M, Prather CM. Gastrointestinal motility problems in the elderly patient. Gastroenterology. 2002; 122(6): 1688–1700.
  6. Drozdowski L, Thomson A. Aging and the intestine. World J Gastroenterol. 2006; 12(47): 7578–7584.
  7. Al-Qudah M. Histological effects of aging on male albino rats’ duodenum. World J Med Sci. 2014; 10(2): 174–178.
  8. Barratt SM, Leeds JS, Robinson K, et al. Reflux and irritable bowel syndrome are negative predictors of quality of life in coeliac disease and inflammatory bowel disease. Eur J Gastroenterol Hepatol. 2011; 23(2): 159–165.
  9. Tosato M, Zamboni V, Ferrini A, et al. The aging process and potential interventions to extend life expectancy. Clin Interv Aging. 2007; 2(3): 401–412.
  10. Møller P, Løhr M, Folkmann JK, et al. Aging and oxidatively damaged nuclear DNA in animal organs. Free Radic Biol Med. 2010; 48(10): 1275–1285.
  11. Kusano C, Ferrari B. Total antioxidant capacity: a biomarker in biomedical and nutritional studies. J Cell Mol Biol. 2008; 7: 1–15.
  12. Smith PD, Smythies LE, Shen R, et al. Intestinal macrophages and response to microbial encroachment. Mucosal Immunol. 2011; 4(1): 31–42.
  13. Singh BN, Shankar S, Srivastava RK. Green tea catechin, epigallocatechin-3-gallate (EGCG): mechanisms, perspectives and clinical applications. Biochem Pharmacol. 2011; 82(12): 1807–1821.
  14. Ferrari CKB. Functional foods, herbs and nutraceuticals: towards biochemical mechanisms of healthy aging. Biogerontology. 2004; 5(5): 275–289.
  15. Chen L, Mo H, Zhao L, et al. Therapeutic properties of green tea against environmental insults. J Nutr Biochem. 2017; 40: 1–13.
  16. Yin Z, Henry EC, Gasiewicz TA. Epigallocatechin-3-gallate is a novel Hsp90 inhibitor. Biochemistry. 2009; 48(2): 336–345.
  17. Murase T, Haramizu S, Ota N, et al. Tea catechin ingestion combined with habitual exercise suppresses the aging-associated decline in physical performance in senescence-accelerated mice. Am J Physiol Regul Integr Comp Physiol. 2008; 295(1): R281–R289.
  18. Gad SB, Zaghloul DM. Beneficial effects of green tea extract on liver and kidney functions, ultrastructure, lipid profile and hematological parameters in aged male rats. Global Vet. 2013; 11(2): 191–205.
  19. Kara A, Unal D, Simsek N, et al. Ultra-structural changes and apoptotic activity in cerebellum of post-menopausal-diabetic rats: a histochemical and ultra-structural study. Gynecol Endocrinol. 2014; 30(3): 226–231.
  20. Bancroft J, Layton C. The Hematoxylin and Eosin. In: Suvarna SK, Layton C, Bancroft JD. ed. Theory and Practice of Histological Techniques. 7th ed. Churchill Livingstone of El Sevier, Philadelphia 2013: 172–214.
  21. Bancroft J, Gamble A. Theory and Practice of Histological Techniques. 6th edition. Churchill Livingstone, New York, London 2008: 225–249.
  22. Karaca T, Şimşek N, Uslu S, et al. The effect of royal jelly on CD3(+), CD5(+), CD45(+) T-cell and CD68(+) cell distribution in the colon of rats with acetic acid-induced colitis. Allergol Immunopathol (Madr). 2012; 40(6): 357–361.
  23. Hayat MA. Principles and techniques of electron microscopy: biological applications. 4th ed. Cambridge University Press, Cambridge, United Kingdom 2000: 4–85.
  24. Giblot Ducray HA, Globa L, Pustovyy O, et al. Mitigation of heat stress-related complications by a yeast fermentate product. J Therm Biol. 2016; 60: 26–32.
  25. Foligne B, Sénégas-Balas F, Antoine JM, et al. Trophic status of the small intestine in young and aged rats: modulation by a yogurt-supplemented diet. Dig Dis Sci. 2004; 49(7-8): 1291–1301.
  26. Baum B, Meneses F, Kleinschmidt S, et al. Age-related histomorphologic changes in the canine gastrointestinal tract: a histologic and immunohistologic study. World J Gastroenterol. 2007; 13(1): 152–157.
  27. Martin K, Kirkwood TB, Potten CS. Age changes in stem cells of murine small intestinal crypts. Exp Cell Res. 1998; 241(2): 316–323.
  28. Holt PR, Pascal RR, Kotler DP. Effect of aging upon small intestinal structure in the Fischer rat. J Gerontol. 1984; 39(6): 642–647.
  29. Thomson ABR. Small intestinal disorders in the elderly. Best Pract Res Clin Gastroenterol. 2009; 23(6): 861–874.
  30. Gessner DK, Bonarius M, Most E, et al. Effects of dietary polyphenol-rich plant products from grape or hop on pro-inflammatory gene expression in the intestine, nutrient digestibility and faecal microbiota of weaned pigs. BMC Vet Res. 2014; 10(4): 196–284.
  31. Frejnagel S, Wroblewska M. Comparative effect of green tea, chokeberry and honeysuckle polyphenols on nutrients and mineral absorption and digestibility in rats. Ann Nutr Metab. 2010; 56(3): 163–169.
  32. Karaca T, Uslu S, Yörük M. Effects of green tea and ginseng on villus length and crypt. Depth and on the distribution of mast and goblet cells in the small intestine of rats with streptozotocin (STZ)-induced diabetes. Philipp J Vet Med. 2011; 48(2): 86–94.
  33. Kang JM, Kim N, Kim JH, et al. Effect of aging on gastric mucosal defense mechanisms: ROS, apoptosis, angiogenesis, and sensory neurons. Am J Physiol Gastrointest Liver Physiol. 2010; 299(5): G1147–G1153.
  34. Newton JL. Changes in upper gastrointestinal physiology with age. Mech Ageing Dev. 2004; 125(12): 867–870.
  35. Rutter K, Sell DR, Fraser N, et al. Green tea extract suppresses the age-related increase in collagen crosslinking and fluorescent products in C57BL/6 mice. Int J Vitam Nutr Res. 2003; 73(6): 453–460.
  36. Holt PR, Yeh Ky. Small intestinal crypt cell proliferation rates are increased in senescent rats. J Gerontol. 1989; 44(1): B9–B14.
  37. Xiao ZQ, Moragoda L, Jaszewski R, et al. Aging is associated with increased proliferation and decreased apoptosis in the colonic mucosa. Mech Ageing Dev. 2001; 122(15): 1849–1864.
  38. Hsu S, Lewis J, Singh B, et al. Green tea polyphenol targets the mitochondria in tumor cells inducing caspase 3-dependent apoptosis. Anticancer Res. 2003; 23(2B): 1533–1539.
  39. Mikkelsen HB, Rumessen JJ. Characterization of macrophage-like cells in the external layers of human small and large intestine. Cell Tissue Res. 1992; 270(2): 273–279.
  40. Kleinschmidt S, Meneses F, Nolte I, et al. Distribution of mast cell subtypes and immune cell populations in canine intestines: evidence for age-related decline in T cells and macrophages and increase of IgA-positive plasma cells. Res Vet Sci. 2008; 84(1): 41–48.
  41. Jang I, Jung K, Cho J. Influence of age on duodenal brush border membrane and specific activities of brush border membrane enzymes in Wistar rats. Exp Anim. 2000; 49(4): 281–287.
  42. Skrzydlewska E, Ostrowska J, Farbiszewski R, et al. Protective effect of green tea against lipid peroxidation in the rat liver, blood serum and the brain. Phytomedicine. 2002; 9(3): 232–238.
  43. Yu BP. Membrane alteration as a basis of aging and the protective effects of calorie restriction. Mech Ageing Dev. 2005; 126(9): 1003–1010.
  44. Łuczaj W, Zapora E, Skrzydlewska E. Influence of green tea on erythrocytes antioxidant status of different age rats intoxicated with ethanol. Phytother Res. 2010; 24(3): 424–428.
  45. El-Beshbishy H. Hepatoprotective effect of green tea (Camellia sinensis) extract against tamoxifen-induced liver injury in rats. BMB Reports. 2005; 38(5): 563–570.
  46. Yang CS, Sang S, Lambert JD, et al. Possible mechanisms of the cancer-preventive activities of green tea. Mol Nutr Food Res. 2006; 50(2): 170–175.
  47. Ren Wy, Wu Kf, Li Xi, et al. Age-related changes in small intestinal mucosa epithelium architecture and epithelial tight junction in rat models. Aging Clin Exp Res. 2014; 26(2): 183–191.
  48. Mabbott NA. A breakdown in communication? Understanding the effects of aging on the human small intestine epithelium. Clin Sci (Lond). 2015; 129(7): 529–531.
  49. Tran L, Greenwood-Van Meerveld B. Age-associated remodeling of the intestinal epithelial barrier. J Gerontol A Biol Sci Med Sci. 2013; 68(9): 1045–1056.
  50. Zhang JB, Du XG, Zhang H, et al. Breakdown of the gut barrier in patients with multiple organ dysfunction syndrome is attenuated by continuous blood purification: effects on tight junction structural proteins. Int J Artif Organs. 2010; 33(1): 5–14.
  51. Suzuki T, Hara H. Role of flavonoids in intestinal tight junction regulation. J Nutr Biochem. 2011; 22(5): 401–408.

Regulations

Important: This website uses cookies. More >>

The cookies allow us to identify your computer and find out details about your last visit. They remembering whether you've visited the site before, so that you remain logged in - or to help us work out how many new website visitors we get each month. Most internet browsers accept cookies automatically, but you can change the settings of your browser to erase cookies or prevent automatic acceptance if you prefer.

By VM Media Group sp z o.o., ul. Świętokrzyska 73, 80–180 Gdańsk

tel.:+48 58 320 94 94, faks:+48 58 320 94 60, e-mail:  viamedica@viamedica.pl